FDA 510(k), K002571, MULITPLE MALE LATX CONDOM
FDA 510(k), K002571, MULITPLE MALE LATX CONDOM
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510(K) Number: K002571
Device Name: MULITPLE MALE LATX CONDOM
Manufacturer: PLEASURE LATEX PRODUCTS SDN. BHD.
Device Classification Name: condom
Regulation Number: 884.5300
Classification Product Code: HIS
Date Received: 08/18/2000
Decision Date: 11/16/2000
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: MULITPLE MALE LATX CONDOM
Manufacturer: PLEASURE LATEX PRODUCTS SDN. BHD.
Device Classification Name: condom
Regulation Number: 884.5300
Classification Product Code: HIS
Date Received: 08/18/2000
Decision Date: 11/16/2000
Regulation Medical Specialty: Obstetrics/Gynecology
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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